BMC Microbiology | |
Functional genomics to identify the factors contributing to successful persistence and global spread of an antibiotic resistance plasmid | |
Laura JV Piddock1  Mark A Webber1  Howard TH Saw1  Jennifer L Cottell1  | |
[1] Institute of Microbiology and Infection, School of Immunity and Infection, The College of Medical and Dental Sciences, The University of Birmingham, Birmingham B15 2TT, UK | |
关键词: Recombination; Plasmid; Mobile genetic element; ESBL; Beta-lactam; | |
Others : 821319 DOI : 10.1186/1471-2180-14-168 |
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received in 2014-02-27, accepted in 2014-06-19, 发布年份 2014 | |
【 摘 要 】
Background
The spread of bacterial plasmids is an increasing global problem contributing to the widespread dissemination of antibiotic resistance genes including β-lactamases. Our understanding of the details of the biological mechanisms by which these natural plasmids are able to persist in bacterial populations and are able to establish themselves in new hosts via conjugative transfer is very poor. We recently identified and sequenced a globally successful plasmid, pCT, conferring β-lactam resistance.
Results
Here, we investigated six plasmid encoded factors (tra and pil loci; rci shufflon recombinase, a putative sigma factor, a putative parB partitioning gene and a pndACB toxin-antitoxin system) hypothesised to contribute to the ‘evolutionary success’ of plasmid pCT. Using a functional genomics approach, the role of these loci was investigated by systematically inactivating each region and examining the impact on plasmid persistence, conjugation and bacterial host biology. While the tra locus was found to be essential for all pCT conjugative transfer, the second conjugation (pil) locus was found to increase conjugation frequencies in liquid media to particular bacterial host recipients (determined in part by the rci shufflon recombinase). Inactivation of the pCT pndACB system and parB did not reduce the stability of this plasmid.
Conclusions
Our findings suggest the success of pCT may be due to a combination of factors including plasmid stability within a range of bacterial hosts, a lack of a fitness burden and efficient transfer rates to new bacterial hosts rather than the presence of a particular gene or phenotype transferred to the host. The methodology used in our study could be applied to other ‘successful’ globally distributed plasmids to discover the role of currently unknown plasmid backbone genes or to investigate other factors which allow these elements to persist and spread.
【 授权许可】
2014 Cottell et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
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20140712072813798.pdf | 436KB | download | |
Figure 2. | 51KB | Image | download |
Figure 1. | 39KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
【 参考文献 】
- [1]Johnson TJ, Nolan LK: Pathogenomics of the virulence plasmids of Escherichia coli. Microbiol Mol Biol Rev 2009, 73(4):750-774.
- [2]van Hoek AH, Mevius D, Guerra B, Mullany P, Roberts AP, Aarts HJ: Acquired antibiotic resistance genes: an overview. Front Microbiol 2011, 2:203.
- [3]Hawkey PM, Jones AM: The changing epidemiology of resistance. J Antimicrob Chemother 2009, 64(suppl 1):i3-i10.
- [4]Piddock LJV: The crisis of no new antibiotics—what is the way forward? Lancet Infect Dis 2012, 12(3):249-253.
- [5]Hawkey PM: The growing burden of antimicrobial resistance. J Antimicrob Chemother 2008, 62(Suppl 1):i1-i9.
- [6]Walsh TR, Weeks J, Livermore DM, Toleman MA: Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: An environmental point prevalence study. Lancet Infect Dis 2011, 11(5):355-362.
- [7]Woodford N, Carattoli A, Karisik E, Underwood A, Ellington MJ, Livermore DM: Complete nucleotide sequences of plasmids pEK204, pEK499, and pEK516, encoding CTX-M enzymes in three major Escherichia coli lineages from the United Kingdom, all belonging to the international O25:H4-ST131 clone. Antimicrob Agents Chemother 2009, 53(10):4472-4482.
- [8]Genome pages - plasmid http://www.ebi.ac.uk/genomes/plasmid.html webcite
- [9]Turner PE, Cooper VS, Lenski RE: Tradeoff between horizontal and vertical modes of transmission in bacterial plasmids. Evolution 1998, 52(2):315-329.
- [10]Hayes F: Toxins-antitoxins: plasmid maintenance, programmed cell death, and cell cycle arrest. Science 2003, 301(5639):1496-1499.
- [11]Dahlberg C, Chao L: Amelioration of the cost of conjugative plasmid carriage in Eschericha coli K12. Genetics 2003, 165(4):1641-1649.
- [12]Salje J: Plasmid segregation: how to survive as an extra piece of DNA. Crit Rev Biochem Mol Biol 2010, 45(4):296-317.
- [13]Dudley EG, Abe C, Ghigo JM, Latour-Lambert P, Hormazabal JC, Nataro JP: An IncI1 plasmid contributes to the adherence of the atypical enteroaggregative Escherichia coli strain C1096 to cultured cells and abiotic surfaces. Infect Immun 2006, 74(4):2102-2114.
- [14]Waters VL: Conjugative transfer in the dissemination of beta-lactam and aminoglycoside resistance. Front Biosci 1999, 4:D433-D456.
- [15]Cottell JL, Webber MA, Coldham NG, Taylor DL, Cerdeno-Tarraga AM, Hauser H, Thomson NR, Woodward MJ, Piddock LJ: Complete sequence and molecular epidemiology of IncK epidemic plasmid encoding blaCTX-M-14. Emerg Infect Dis 2011, 17(4):645-652.
- [16]Liebana E, Batchelor M, Hopkins KL, Clifton-Hadley FA, Teale CJ, Foster A, Barker L, Threlfall EJ, Davies RH: Longitudinal farm study of extended-spectrum beta-lactamase-mediated resistance. J Clin Microbiol 2006, 44(5):1630-1634.
- [17]Teale CJ, Barker L, Foster AP, Liebana E, Batchelor M, Livermore DM, Threlfall EJ: Extended-spectrum beta-lactamase detected in E coli recovered from calves in Wales. Vet Rec 2005, 156(6):186-187.
- [18]Cottell JL, Webber MA, Piddock LJ: Persistence of transferable ESBL resistance in the absence of antibiotic pressure. Antimicrob Agents Chemother 2012, 56(9):4703-4706.
- [19]Thomason LC, Costantino N, Shaw DV, Court DL: Multicopy plasmid modification with phage lambda Red recombineering. Plasmid 2007, 58(2):148-158.
- [20]Nielsen AK, Gerdes K: Mechanism of post-segregational killing by hok-homologue pnd of plasmid R483: two translational control elements in the pnd mRNA. J Mol Biol 1995, 249(2):270-282.
- [21]Bradley DE: Characteristics and function of thick and thin conjugative pili determined by transfer-derepressed plasmids of incompatibility groups I1, I2, I5, B, K and Z. J Gen Microbiol 1984, 130(6):1489-1502.
- [22]Komano T, Kim SR, Yoshida T: Mating variation by DNA inversions of shufflon in plasmid R64. Adv Biophys 1995, 31:181-193.
- [23]Sharan SK, Thomason LC, Kuznetsov SG, Court DL: Recombineering: a homologous recombination-based method of genetic engineering. Nat Protoc 2009, 4(2):206-223.
- [24]Furuya N, Komano T: Nucleotide sequence and characterization of the trbABC region of the IncI1 plasmid R64: existence of the pnd gene for plasmid maintenance within the transfer region. J Bacteriol 1996, 178(6):1491-1497.
- [25]Friedman SA, Austin SJ: The P1 plasmid-partition system synthesizes two essential proteins from an autoregulated operon. Plasmid 1988, 19(2):103-112.
- [26]Komano T, Yoshida T, Narahara K, Furuya N: The transfer region of IncI1 plasmid R64: similarities between R64 tra and Legionella icm/dot genes. Mol Microbiol 2000, 35(6):1348-1359.
- [27]Yoshida T, Kim SR, Komano T: Twelve pil genes are required for biogenesis of the R64 thin pilus. J Bacteriol 1999, 181(7):2038-2043.
- [28]Call DR, Singer RS, Meng D, Broschat SL, Orfe LH, Anderson JM, Herndon DR, Kappmeyer LS, Daniels JB, Besser TE: blaCMY-2-positive IncA/C plasmids from Escherichia coli and Salmonella enterica are a distinct component of a larger lineage of plasmids. Antimicrob Agents Chemother 2010, 54(2):590-596.
- [29]Potron A, Poirel L, Nordmann P: Plasmid-mediated transfer of the blaNDM-1 gene in Gram-negative rods. FEMS Microbiol Lett 2011, 324(2):111-116.
- [30]Datsenko KA, Wanner BL: One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products. Proc Natl Acad Sci U S A 2000, 97(12):6640-6645.
- [31]Hartskeerl R, Zuidweg E, van Geffen M, Hoekstra W: The IncI plasmids R144, R64 and ColIb belong to one exclusion group. J Gen Microbiol 1985, 131(6):1305-1311.
- [32]Baugh S, Ekanayaka AS, Piddock LJ, Webber MA: Loss of or inhibition of all multidrug resistance efflux pumps of Salmonella enterica serovar Typhimurium results in impaired ability to form a biofilm. J Antimicrob Chemother 2012, 67(10):2409-2417.
- [33]Webber MA, Randall LP, Cooles S, Woodward MJ, Piddock LJV: Triclosan resistance in Salmonella enterica serovar Typhimurium. J Antimicrob Chemother 2008, 62(1):83-91.
- [34]Pope CF, Gillespie SH, Moore JE, McHugh TD: Approaches to measure the fitness of Burkholderia cepacia complex isolates. J Med Microbiol 2010, 59(Pt 6):679-686.